Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H29N3O2 |
| Molecular Weight | 319.4418 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNC(=O)NCCCOC1=CC=CC(CN2CCCCC2)=C1
InChI
InChIKey=SVCQBXMFONNZHX-UHFFFAOYSA-N
InChI=1S/C18H29N3O2/c1-2-19-18(22)20-10-7-13-23-17-9-6-8-16(14-17)15-21-11-4-3-5-12-21/h6,8-9,14H,2-5,7,10-13,15H2,1H3,(H2,19,20,22)
| Molecular Formula | C18H29N3O2 |
| Molecular Weight | 319.4418 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/8096132Curator's Comment: description was created based on several sources, including, http://www.ncbi.nlm.nih.gov/pubmed/8096133,
http://www.ncbi.nlm.nih.gov/pubmed/8096134
Sources: http://www.ncbi.nlm.nih.gov/pubmed/8096132
Curator's Comment: description was created based on several sources, including, http://www.ncbi.nlm.nih.gov/pubmed/8096133,
http://www.ncbi.nlm.nih.gov/pubmed/8096134
Dalcotidine is a histamine H2 receptor antagonist that demonstrated potent gastric mucosal protective activity on acute gastric lesions and duodenal ulcers. Dalcotidine was discontinued in phase III of clinical trials in Japan.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P25021 Gene ID: 3274.0 Gene Symbol: HRH2 Target Organism: Homo sapiens (Human) Sources: http://www.ncbi.nlm.nih.gov/pubmed/8096132 |
0.04 µM [Ki] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Influence of KU-1257 on the recurrence and relapse of acetic acid-induced chronic gastric ulcers in rats]. | 1996-02 |
|
| Pharmacological profiles of the new histamine H2-receptor antagonist N-ethyl-N'-[3-[3-(piperidinomethyl)phenoxy] propyl] urea. | 1993-02 |
|
| Effects of the new histamine H2-receptor antagonist N-ethyl-N'-[3-[3-(piperidinomethyl)phenoxy]propyl] urea with potent gastric mucosal protective activity on acute gastric lesions and duodenal ulcers in rats. | 1993-02 |
|
| Healing-promoting action of the new histamine H2-receptor antagonist N-ethyl-N'-[3-[3-(piperidinomethyl)phenoxy]propyl]urea with dual action on chronic gastric and duodenal ulcers induced by acetic acid in rats. | 1993-02 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/8096134
Curator's Comment: No human-related information is found.
In rats: 10-50 mg/kg x 2/day
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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on
Edited
Mon Mar 31 18:31:39 GMT 2025
by
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| Record UNII |
9968S2UKFJ
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C29702
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C73218
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